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2003 | 50 | 4 | 1195-1203

Article title

Analysis of microsatellite instability and loss of heterozygosity in breast cancer with the use of a well characterized multiplex system.

Content

Title variants

Languages of publication

EN

Abstracts

EN
Analysis of microsatellite instability (MI) and loss of heterozygosity (LOH) is recommended for screening patients with sporadic and hereditary malignancies. This study shows an application of a fluorescent hexaplex PCR system for microsatellite typing on A.L.F. DNA Sequencer (Pharmacia Biotech). This technique detects changes in microsatellites providing a time-efficient, reliable and accurate method for MI and LOH analyses. The Fragment Manager software was used for automated size calculation and quantitation of DNA fragments, enabling rapid and precise measurement of allelic ratios. We examined 70 breast cancer and 70 control DNA specimens, classified all the patterns of microsatellite alterations, and set up MI and LOH assessment criteria for the automated multiplex fluorescent method.

Year

Volume

50

Issue

4

Pages

1195-1203

Physical description

Dates

published
2003
revised
2003-07-09
accepted
2003-08-18
received
2003-12-10

Contributors

  • Department of Human Biology, The Ludwik Rydygier Medical University of Bydgoszcz, Bydgoszcz, Poland
  • Forensic Medicine Institute, The Ludwik Rydygier Medical University of Bydgoszcz, Bydgoszcz, Poland
author
  • Forensic Medicine Institute, The Ludwik Rydygier Medical University of Bydgoszcz, Bydgoszcz, Poland
  • Forensic Medicine Institute, The Ludwik Rydygier Medical University of Bydgoszcz, Bydgoszcz, Poland
  • Forensic Medicine Institute, The Ludwik Rydygier Medical University of Bydgoszcz, Bydgoszcz, Poland
author
  • Department of Human Biology, The Ludwik Rydygier Medical University of Bydgoszcz, Bydgoszcz, Poland
  • Regional Center of Oncology, Bydgoszcz, Poland
author
  • Regional Center of Oncology, Bydgoszcz, Poland

References

  • Aaltonen LA, Peltomaki P, Leach FS, Sistonene P, Pylkkanen L, Mecklin JP, Jarvinen H, Powell SM, Jen J, Hamilton SR, Peterson GM, Kinzler KW, Vogelstein B, de la Chapelle A. (1993) Clues to the pathogenesis of familial colorectal cancer. Science.; 260: 812-6.
  • Aaltonen LA, Aslovaara MD, Kristo P, Canzian F, Hemminki A, Peltomaki P, Chadwick RB, Kaariainen H, Eskelinen MD, Jarvinen H, Mecklin JP, Chapelle A. (1998) Incidence of hereditary nonpolyposis colorectal cancer and the feasibility of molecular screening for the disease. N Engl J Med.; 338: 1481-7.
  • Aldaz CM, Chen T, Sahin A, Cunningham J, Bondy M. (1995) Comparative allelotype of in situ and invasive human breast cancer: high frequency of microsatellite instability in lobular breast carcinomas. Cancer Res.; 55: 3976-81.
  • Arzimanoglou II, Gilbert F, Barber HRK. (1998) Microsatellite instability in human solid tumors. Cancer.; 82: 1808-20.
  • Bièche I, Lidereau R. (1995) Genetic alteration in breast cancer. Genes Chromosomes Cancer.; 14: 227-51.
  • Bronner CE, Baker SM, Morrison PT, Warren G, Smith LG, Lescoe MK, Kane M, Earabino C, Lipford J, Lindblom A, Tannergard P, Bollag RJ, Godwin AR, Ward DC, Nodenskjold M, Fishel R, Kolodner R, Liskay RM. (1994) Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary nonpolyposis colon cancer. Nature.; 368: 258-61.
  • De Marchis L, Contegiacomo A, D'Amico C. (1997) Microsatellite instability is correlated with lymph node-positive breast cancer. Clin Cancer Res.; 3: 241-8.
  • Fearon ER, Cho KR, Nigro JM, Kern SE, Simons JW, Ruppert JM, Hamilton SR, Preisinger AC, Thomas G, Kinzler KW. (1990) Identification of a chromosome 18q gene that is altered in colorectal cancer. Science.; 247: 49-56
  • Feunteun J. (1998) Breast cancer and genetic instability: the molecules behind the scenes. Mol Med Today.; 4: 263-7.
  • Feunteun J, Lenoir GM. (1996) BRCA1, a gene involved in inherited predisposition to breast and ovarian cancer. Biochim Biophys Acta.; 1242: 177-80.
  • Fishel R, Lescoe MK, Rao MR, Copeland NG, Jenkins NA, Garber J, Kane M, Kolodner R. (1993) The human mutator gene homolog MSH2 and association with hereditary nonpolyposis colon cancer. Cell.; 75: 1027-38.
  • Jass JR, Cottier DS, Jeevaratnam P, Pokos V, Holdaway KM, Bowden ML, Van de Water NS, Browett PJ. (1995) Diagnostic use of microsatellite instability in hereditary non-polyposis colorectal cancer. Lancet.; 346: 1200-1.
  • Knudson AG. (1993) Antioncogenes and human cancer. Proc Natl Acad Sci U S A.; 90: 10914-20.
  • Li L, Li X, Franke U, Cohen SN. (1997) The TSG101 tumor susceptibility gene is located in chromosome 11 band p15 and mutated in human breast cancer. Cell.; 88: 143-54.
  • Miścicka-Śliwka D, Grzybowski T, Woźniak M. (1997) Optimization of a hexaplex PCR amplification from Short Tandem Repeats (STR) and amelogenin (AMG) loci. Electrophoresis.; 18: 1627-32.
  • Meuth M. (1990) The structure of mutation in mammalian cells. Biochim Biophys Acta.; 1032: 1-17.
  • Papadopoulos N, Nicolaides NC, Wei YF, Ruben SM, Carter KC, Rosen CA, Haseltine WA, Fleischmann RD, Fraser CM, Adams MD, Venter JC, Hamilton SR, Petersen GM, Watson P, Lynch HT, Peltomaki P, Mecklin JP, de la Chapelle A, Kinzler KW, Volgelstein B. (1994) Mutaton of a mutL homolog in hereditary colon cancer. Science.; 263: 1625-9.
  • Risinger, JI, Barrett JC, Watson P. Lynch HT, Boyd J. (1996) Molecular genetic evidence of the occurrence of breast cancer as an integral tumor in patients with the hereditary nonpolyposis colorectal carcinoma syndrome. Cancer.; 77: 1836-43.
  • Sambrook J, Fritsch EF, Maniatis T. (1989) Analysis and cloning of eucaryotic genomic DNA. In Molecular cloning, a labolatory manual. pp 16-22. Cold Spring Harbor Laboratory Press.
  • Sidransky D. (1997) Nucleid acid-based method for the detection of cancer. Science.; 278: 1054-8.
  • Sobczak K, Kozłowski P, Napierała M, Czarny J, Woźniak M, Kapuścińska K, Łośko M, Koziczak M, Jasińska A, Powierska J, Braczkowski R, Bręborowicz J, Godlewski D, Mackiewicz A, Krzyżosiak W. (1997) Novel BRCA1 mutations and more frequent intron-20 alteration found among 236 women from Western Poland. Oncogene.; 15: 1773-9.
  • Sourvinos G, Kiaris H, Tsikkinis A, Vassilaros S, Spandidos DA. (1997) Microsatellite instability and loss of heterozygosity in primary breast cancer. Tumour Biol.; 18: 157-66.
  • Toh Y, Oki E, Oda S, Tomoda M, Tomisaki S, Ichiyoshi Y, Ohno S, Sugimachi K. (1996) An integrated microsatellite length analysis using automated fluorescent DNA sequencer. Cancer Res.; 56: 2688-91.
  • Wang Y, Hung S, Linn JF, Steiner G, Glazer AN, Sidransky D, Mathies RA. (1997) Microsatellite-based cancer detection using capillary array electrophoresis and energy-transfer fluorescent primers. Electrophoresis.; 18: 1742-9.
  • Wooster R, Cleton-Jansen AM, Collins N, Mangion J, Cornelis RS, Cooper CS, Gusterson BA, Ponder BA, von Deimling A, Wiestler OD. (1994) Instability of short tandem repeats in human cancer. Nat Genet.; 6: 152-6.
  • Wooster R, Neuhausen SL, Mangion J, Quirk Y, Ford D, Collins N, Nguyen K, Seal S, Tran T, Averill D, Fields P, Marshall G, Narod S, Lenoir GM, Lynch H, Feunteun J, Odevilee P, Cornelisse CJ, Menko FH, Daly PA, Ormiston W, McManus R, Pye C, Lewis CM, Cannon-Albright LA, Petro J, Ponder BAJ, Skolnik MH, Easton DF, Goldgar DE, Stratton MR. (1994) Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13. Science.; 265: 2088-90.
  • Yee CJ, Roodi N, Verrier CS, Parl FF. (1994) Microsatellite instability and loss of heterozygosity in breast cancer. Cancer Res.; 54: 1641-4.

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.bwnjournal-article-abpv50i4p1195kz
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